Package 60760-956-90

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-956-90
Digits Only 6076095690
Product NDC 60760-956
Description

90 TABLET in 1 BOTTLE, PLASTIC (60760-956-90)

Marketing

Marketing Status
Marketed Since 2025-08-19
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ca9e2b4-da38-7408-e063-6294a90a0057", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049611"], "spl_set_id": ["3ca9f0d9-a40d-4416-e063-6394a90aec8b"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-956-30)", "package_ndc": "60760-956-30", "marketing_start_date": "20250819"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (60760-956-60)", "package_ndc": "60760-956-60", "marketing_start_date": "20250819"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-956-90)", "package_ndc": "60760-956-90", "marketing_start_date": "20250819"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "60760-956_3ca9e2b4-da38-7408-e063-6294a90a0057", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60760-956", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA077712", "marketing_category": "ANDA", "marketing_start_date": "20240910", "listing_expiration_date": "20261231"}